Skip to main content
Log in

Evidence for the involvement of cell wall peroxidase in the generation of hydroxyl radicals mediating extension growth

  • Original Article
  • Published:
Planta Aims and scope Submit manuscript

Abstract

Hydroxyl radicals (·OH), produced in the cell wall, are capable of cleaving wall polymers and can thus mediate cell wall loosening and extension growth. It has recently been proposed that the biochemical mechanism responsible for ·OH generation in the cell walls of growing plant organs represents an enzymatic reaction catalyzed by apoplastic peroxidase (POD). This hypothesis was investigated by supplying cell walls of maize (Zea mays L.) coleoptiles and sunflower (Helianthus annuus L.) hypocotyls with external NADH, an artificial substrate known to cause ·OH generation by POD in vitro. The effects of NADH on wall loosening, growth, and ·OH production in vivo were determined. NADH mediates cell wall extension in vitro and in vivo in an H2O2-dependent reaction that shows the characteristic features of POD. NADH-mediated production of ·OH in vivo was demonstrated in maize coleoptiles using electron paramagnetic resonance spectroscopy in combination with a specific spin-trapping reaction. Kinetic properties and inhibitor/activator sensitivities of the ·OH-producing reaction in the cell walls of coleoptiles resembled the properties of horseradish POD. Apoplastic consumption of external NADH by living coleoptiles can be traced back to the superimposed action of two enzymatic reactions, a KCN-sensitive reaction mediated by POD operating in the ·OH-forming mode, and a KCN-insensitive reaction with the kinetic properties of a superoxide-producing plasma-membrane NADH oxidase the activity of which can be promoted by auxin. Under natural conditions, i.e. in the absence of external NADH, this enzyme may provide superoxide (O2 ·) (and H2O2 utilized by POD for) ·OH production in the cell wall.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Institutional subscriptions

Fig. 1.
Fig. 2.
Fig. 3a, b.
Fig. 4.
Fig. 5.
Fig. 6.
Fig. 7a, b.
Fig. 8.
Fig. 9.
Fig. 10.
Fig. 11.
Fig. 12.
Fig. 13.

Similar content being viewed by others

Abbreviations

CAT:

catalase

2,4-D:

2,4-dichlorophenoxyacetate

DCP:

2,4-dichlorophenol

EPR:

electron paramagnetic resonance

HRP:

horseradish peroxidase

IAA:

indole-3-acetate

Mn-DFA:

manganese-desferrioxamine

Mn-TMP:

manganese-tetrakis(methylpyridyl)porphine

POBN:

α-(4-pyridyl-1-oxide)-N-tert-butylnitrone

POD:

peroxidase

SOD:

superoxide dismutase

References

  • Akazawa T, Conn EE (1958) The oxidation of reduced pyridine nucleotides by peroxidase. J Biol Chem 232:403–415

    CAS  Google Scholar 

  • Barr R, Morré DJ, Crane FL (2000) Oxidation of NADH by hypocotyl segments from soybean is stimulated by 2,4-D. Plant Physiol Biochem 38:739–745

    Article  CAS  Google Scholar 

  • Beyer WF, Fridovich I (1989) Characterization of a superoxide dismutase mimic prepared from desferrioxamine and MnO2. Arch Biochem Biophys 271:149–156

    CAS  PubMed  Google Scholar 

  • Buettner GR (1987) Spin trapping: ESR parameters of spin adducts. Free Radic Biol Med 3:259–303

    CAS  PubMed  Google Scholar 

  • Chance B, Maehly AC (1955) Assay of catalases and peroxidases. Methods Enzymol 2:764–775

    Google Scholar 

  • Chen S-X, Schopfer P (1999) Hydroxyl-radical production in physiological reactions. A novel function of peroxidase. Eur J Biochem 260:726–735

    Article  CAS  PubMed  Google Scholar 

  • Cosgrove DJ (2001) Wall structure and wall loosening. A look backwards and forwards. Plant Physiol 125:131–134

    Article  CAS  PubMed  Google Scholar 

  • Day BJ, Crapo JD (1996) A metalloporphyrin superoxide dismutase mimetic protects against paraquat-induced lung injury in vivo. Toxicol Appl Pharmacol 140:94–100

    Google Scholar 

  • Day BJ, Fridovich I, Crapo JD (1997) Manganic porphyrins possess catalase activity and protect endothelial cells against hydrogen peroxide-mediated injury. Arch Biochem Biophys 347:256–262

    Article  CAS  PubMed  Google Scholar 

  • De Sandro V, Dupny C, Kaniewski J, Ohayon R, Dème D, Virion A, Pommier J (1991) Mechanism of NADPH oxidation catalyzed by horse-radish peroxidase and 2,4-diacetyl-[2H]heme-substituted horse-radish peroxidase. Eur J Biochem 201:507–513

    PubMed  Google Scholar 

  • DeHahn T, Barr R, Morré DJ (1997) NADH oxidase activity present on both the external and internal surfaces of soybean plasma membranes. Biochim Biophys Acta 1328:99–108

    Article  CAS  Google Scholar 

  • Frahry G, Schopfer P (2001) NADH-stimulated, cyanide-resistant superoxide production in maize coleoptiles analyzed with a tetrazolium-based assay. Planta 212:175–183

    CAS  PubMed  Google Scholar 

  • Fry SC (1998) Oxidative scission of plant cell wall polysaccharides by ascorbate-induced hydroxyl radicals. Biochem J 332:507–515

    CAS  PubMed  Google Scholar 

  • Giandomenico AR, Cerniglia GE, Biaglow JE, Stevens CW, Koch CJ (1997) The importance of sodium pyruvate in assessing damage produced by hydrogen peroxide. Free Radic Biol Med 23:426–434

    Article  CAS  PubMed  Google Scholar 

  • Halliwell B (1978) Lignin synthesis: the generation of hydrogen peroxide and superoxide by horseradish peroxidase and its stimulation by manganese(II) and phenols. Planta 140:81–88

    CAS  Google Scholar 

  • Halliwell B, Gutteridge JMC (1999) Free radicals in biology and medicine. 3rd edn. Oxford University Press, Oxford

  • Hicks C, Morré DJ (1998) Oxidation of NADH by intact segments of soybean hypocotyls and stimulation by 2,4-D. Biochim Biophys Acta 1375:1-5

    Article  CAS  PubMed  Google Scholar 

  • Hohl M, Schopfer P (1992) Physical extensibility of maize coleoptile cell walls: apparent plastic extensibility in due to elastic hysteresis. Planta 187:498–504

    Google Scholar 

  • Kawano T, Kawano N, Muto S, Lapeyrie F (2002) Retardation and inhibition of the cation-induced superoxide generation in BY-2 tobacco cell suspension culture by Zn2+ and Mn2+. Physiol Plant 114:395–404

    Article  CAS  PubMed  Google Scholar 

  • Kutschera U, Schopfer P (1985) Evidence against the acid-growth theory of auxin action. Planta 163:483–493

    CAS  Google Scholar 

  • Lin W (1982) Responses of corn root protoplasts to exogenous reduced nicotinamide adenine dinucleotide: oxygen consumption, ion uptake and membrane potential. Proc Natl Acad Sci USA 79:3773–3776

    CAS  Google Scholar 

  • Michot JL, Virion A, Dème D, De Prailaune S, Pommier J (1985) NADPH oxidation catalyzed by the peroxidase/H2O2 system. Guaiacol-mediated and scopoletin-mediated oxidation of NADPH to NADP+. Eur J Biochem 148:441–445

    CAS  PubMed  Google Scholar 

  • Penel C, Castillo FJ (1991) Peroxidases of plasma membranes, apoplastic ascorbate, and relation of redox activities to plant pathology. In: FL Crane, DJ Morré, HE Löw (eds) Oxidation at the plasma membrane: relation to growth and transport, vol II. CRC Press, Boca Raton, FL, pp 122–147

    Google Scholar 

  • Ramos CL, Pou S, Britigan BE, Cohen MS, Rosen GM (1992) Spin trapping evidence for myeloperoxidase-dependent hydroxyl radical formation by human neutrophils and monocytes. J Biol Chem 267:8307–8312

    CAS  PubMed  Google Scholar 

  • Rosen GM, Rauckman EJ (1984) Spin trapping of superoxide and hydroxyl radicals. Methods Enzymol 105:198–209

    CAS  PubMed  Google Scholar 

  • Schopfer P (1993) Determination of auxin-dependent pH changes in coleoptile cell walls by a null-point method. Plant Physiol 103:351–357

    CAS  PubMed  Google Scholar 

  • Schopfer P (2001) Hydroxyl radical-induced cell-wall loosening in vitro and in vivo: implications for the control of elongation growth. Plant J 28:679–688

    Article  CAS  PubMed  Google Scholar 

  • Schopfer P, Liszkay A, Bechtold M, Frahry G, Wagner A (2002) Evidence that hydroxyl radicals mediate auxin-induced extension growth. Planta 214:821–828

    Article  CAS  PubMed  Google Scholar 

  • Schweikert C, Liszkay A, Schopfer P (2000) Scission of polysaccharides by peroxidase-generated hydroxyl radicals. Phytochemistry 53:565–570

    Article  CAS  PubMed  Google Scholar 

  • Schweikert C, Liszkay A, Schopfer P (2002) Polysaccharide degradation by Fenton reaction- or peroxidase-generated hydroxyl radicals in isolated plant cell walls. Phytochemistry 61:31–35

    Article  CAS  PubMed  Google Scholar 

  • Suzuki H, Pabst MJ, Johnston RB (1985) Enhancement by Ca2+ or Mg2+ of catalytic activity of the superoxide-producing NADPH oxidase in membrane fractions of human neutrophils and monocytes. J Biol Chem 260:3635–3639

    CAS  PubMed  Google Scholar 

  • Vianello A, Macri F (1989) NAD(P)H oxidation elicits anion superoxide formation in radish plasmalemma vesicles. Biochim Biophys Acta 980:202–208

    CAS  PubMed  Google Scholar 

  • Vianello A, Macri F (1991) Generation of superoxide anion and hydrogen peroxide at the surface of plant cells. J Bioenerg Biomembr 23:409–423

    CAS  PubMed  Google Scholar 

  • Yamazaki I, Yokota K (1973) Oxidation states of peroxidase. Mol Cell Biochem 2:39–52

    CAS  PubMed  Google Scholar 

  • Yokota K, Yamazaki I (1965) Reaction of peroxidase with reduced nicotinamide-adenine dinucleotide and nicotinamide-adenine dinucleotide phosphate. Biochim Biophys Acta 105:301–312

    CAS  PubMed  Google Scholar 

Download references

Acknowledgement

We thank Bernd Wurst for expert technical assistance.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Peter Schopfer.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Liszkay, A., Kenk, B. & Schopfer, P. Evidence for the involvement of cell wall peroxidase in the generation of hydroxyl radicals mediating extension growth. Planta 217, 658–667 (2003). https://doi.org/10.1007/s00425-003-1028-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-003-1028-1

Keywords

Navigation